Polymerization of ε-Caprolactone Using Bis(phenoxy)-amine Aluminum Complex: Deactivation by Lactide

被引:13
作者
Chumsaeng, Phongnarin [1 ]
Haesuwannakij, Setsiri [2 ]
Bureekaew, Sareeya [3 ]
Ervithayasuporn, Vuthichai [1 ]
Namuangruk, Supawadee [4 ]
Phomphrai, Khamphee [2 ]
机构
[1] Mahidol Univ, Fac Sci, Dept Chem, Bangkok 10400, Thailand
[2] Vidyasirimedhi Inst Sci & Technol VISTEC, Sch Mol Sci & Engn, Dept Mat Sci & Engn, Wangchan 21210, Rayong, Thailand
[3] Vidyasirimedhi Inst Sci & Technol VISTEC, Sch Energy Sci & Engn, Dept Chem & Biomol Engn, Wangchan 21210, Rayong, Thailand
[4] Natl Sci & Technol Dev Agcy, Natl Nanotechnol Ctr, Klongluang 12120, Pathumthani, Thailand
关键词
RING-OPENING POLYMERIZATION; ZIRCONIUM COMPLEXES; TITANIUM COMPLEXES; COORDINATION POLYMERIZATION; ISOSPECIFIC POLYMERIZATION; 1-HEXENE POLYMERIZATION; OLEFIN POLYMERIZATION; LIVING POLYMERIZATION; PHENOLATE LIGANDS; CYCLIC ESTERS;
D O I
10.1021/acs.inorgchem.8b01364
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Polymerizations of biodegradable lactide and lactones have been the subjects of intense research during the past decade. They can be polymerized/copolymerized effectively by several catalyst systems. With bis(phenolate)-amine aluminum complex, we have shown for the first time that lactide monomer can deactivate the aluminum complex during the ongoing polymerization of epsilon-caprolactone to a complete stop. After hours of dormant state, the aluminum complex can be reactivated again by heating at 100 degrees C without the addition of any external chemicals still giving polymer with narrow dispersity. Studies using NMR, in situ FTIR, and single-crystal X-ray crystallography indicated that the coordination of the carbonyl group in lactyl unit was responsible for the unusual behavior of lactide. In addition, the unusual methyl-migration from methyl lactate ligand to the amine side chain of the aluminum complex was observed through intermolecular nucleophilic-attack mechanism.
引用
收藏
页码:10170 / 10179
页数:10
相关论文
共 68 条
[21]   Controlled ring-opening polymerization of lactide and glycolide [J].
Dechy-Cabaret, O ;
Martin-Vaca, B ;
Bourissou, D .
CHEMICAL REVIEWS, 2004, 104 (12) :6147-6176
[22]   Single site catalysts for stereoselective ring-opening polymerization of lactides [J].
Dijkstra, Pieter Jelle ;
Du, Hongzhi ;
Feijen, Jan .
POLYMER CHEMISTRY, 2011, 2 (03) :520-527
[23]   Fluorinated bis(phenoxyketimine)titanium complexes for the living, isoselective polymerization of propylene: Multiblock isotactic polypropylene copolymers via sequential monomer addition [J].
Edson, Joseph B. ;
Wang, Zhigang ;
Kramer, Edward J. ;
Coates, Geoffrey W. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (14) :4968-4977
[24]   REACTIONS OF ESTERS WITH TERTIARY AMINES .1. BENZYL ESTERS FROM METHYL ESTERS AND BENZYLDIMETHYLAMINE [J].
ELIEL, EL ;
ANDERSON, RP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1952, 74 (02) :547-549
[25]   UNUSUAL STRUCTURAL FEATURE OF CRYSTALLINE PHTHALIC-ACID [J].
ERMER, O .
HELVETICA CHIMICA ACTA, 1981, 64 (06) :1902-1909
[26]   NMR analysis of low molecular weight poly(lactic acid)s [J].
Espartero, JL ;
Rashkov, I ;
Li, SM ;
Manolova, N ;
Vert, M .
MACROMOLECULES, 1996, 29 (10) :3535-3539
[27]  
Frisch M.J., 2016, GAUSSIAN 16 REV
[28]   Titanium and zirconium complexes of dianionic and trianionic amine - Phenolate-type ligands in catalysis of lactide polymerization [J].
Gendler, Shimrit ;
Segal, Sharon ;
Goldberg, Israel ;
Goldschmidt, Zeev ;
Kol, Moshe .
INORGANIC CHEMISTRY, 2006, 45 (12) :4783-4790
[29]   Advances in non-metallocene olefin polymerization catalysis [J].
Gibson, VC ;
Spitzmesser, SK .
CHEMICAL REVIEWS, 2003, 103 (01) :283-315
[30]   Diverse structure-activity trends in amine bis(phenolate) titanium polymerization catalysts [J].
Groysman, S ;
Tshuva, EY ;
Goldberg, I ;
Kol, M ;
Goldschmidt, Z ;
Shuster, M .
ORGANOMETALLICS, 2004, 23 (22) :5291-5299